HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

hemoglobin Raleigh

beta1(NA1)Val replaced by Ac-Ala; found in Swedish diabetic patients

Also Known As:

Hb Raleigh; Hemoglobin Raleigh

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Blood Proteins: 12459
    - Hemoglobins: 37188
      - Abnormal Hemoglobins: 120
        hemoglobin Raleigh: 2
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        hemoglobin Raleigh: 2

Experts

1.	Chambliss, Allison B: 1 article (09/2021)
2.	Lee, Patricia: 1 article (09/2021)
3.	Marin, Maximo J: 1 article (09/2021)
4.	Agosti, Steven J: 1 article (01/2007)
5.	Man, Mary A: 1 article (01/2007)
6.	Mastorides, Stephen M: 1 article (01/2007)
7.	Thomas, L Brannon: 1 article (01/2007)

Related Diseases

1.	Sickle Cell Trait 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "
2.	Hemoglobinopathies 09/01/2021 - "Hemoglobinopathy testing led to the identification of a hemoglobin variant consistent with Hb Raleigh, in which a valine → alanine substitution on the beta chain effects a charge difference, resulting in coelution with HbA1c on HPLC and a spuriously high reading. "
3.	Sickle Cell Anemia (Hemoglobin S Disease) 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "
4.	Hb C disease 01/01/2007 - "In 252 cases, sickle cell trait was identified with a mean retention time (RT) of 1.44 (SD +/-0.02) min. In 82 cases, Hb C trait was identified with a mean RT of 1.66 +/-0.03 min. RTs for other Hb abnormalities, including sickle cell disease, homozygous Hb C disease, C Harlem trait, alpha-chain Hb variants, Hb D trait, Hb G trait, Hb J trait, Hb Raleigh, and Hb Lepore were also determined. "

Related Drugs and Biologics

1.	Valine (L-Valine)
2.	Hemoglobins (Hemoglobin)
3.	Alanine (L-Alanine)
4.	hemoglobin Lepore
5.	hemoglobin D